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991.
992.
Tatsuya Yanagisawa Hiroyuki Hidaka Hiroshi Amitsuka Shintaro Nakamura Satoshi Awaji Elizabeth L. Green 《哲学杂志》2020,100(10):1268-1281
ABSTRACTIn this study, ultrasonic measurements were performed on a single crystal of cubic PrNi2Cd20, down to a temperature of 0.02?K, to investigate the crystalline electric field ground state and search for possible phase transitions at low temperatures. The elastic constant (C11?C12)/2, which is related to the Γ3-symmetry quadrupolar response, exhibits the Curie-type softening at temperatures below ~30?K, which indicates that the present system has a Γ3 non-Kramers doublet ground state. A leveling-off of the elastic response appears below ~0.1?K toward the lowest temperatures, which implies the presence of level splitting owing to a long-range order in a finite-volume fraction associated with Γ3-symmetry multipoles. A magnetic field–temperature phase diagram of the present compound is constructed up to 28?T for H || [110]. A clear acoustic de Haas–van Alphen signal and a possible magnetic-field-induced phase transition at H ~26?T are also detected by high-magnetic-field measurements. 相似文献
993.
Sergey A. Anufriev Igor B. Sivaev Hiroyuki Nakamura 《Phosphorus, sulfur, and silicon and the related elements》2020,195(11):910-917
AbstractTwo ways of synthesis of theragnostic compounds for Gd-guided boron neutron capture therapy of cancer are proposed. The first way is based on modification of DO3A ligand, which a capable to form stable complexes with gadolinium, with attachment of boron-containing moieties and additional functional groups which can be used for conjugation with various biomacromolecules. The second way is based on the introduction of additional chelating groups into a boron-containing moiety—carborane-based ligand. It is expected that this will significantly improve the stability of the gadolinium bis(dicarbollide) complexes. 相似文献
994.
995.
996.
Ayako Oda Yosuke Suzuki Banri Sato Haruki Sato Ryota Tanaka Hiroyuki Ono Tadasuke Ando Toshitaka Shin Hiromitsu Mimata Hiroki Itoh Keiko Ohno 《Journal of separation science》2022,45(10):1672-1682
Indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid are uremic toxins that accumulate in renal failure and have been reported to decrease the activities of the drug-metabolizing enzyme cytochrome P450 3A and the drug transporter organic anion transporting polypeptides 1B, respectively. In this study, we established and validated an assay for simultaneous quantification of indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid in human plasma. The samples were pretreated by solid-phase extraction, and measured by ultra-high-performance liquid chromatography–tandem mass spectrometry. The validation results for this assay were within the acceptable limits recommended by the US Food and Drug Administration, with a lower limit of quantitation of 0.05 μg/mL for both indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid. Recovery rates of indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid corrected by internal standard were 100.7–101.9 and 100.2–101.3%, respectively. Matrix effects of indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid corrected by internal standard were 101.1–105.5 and 97.0–103.8%, respectively. The validated assay was used to analyze indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid concentrations in the plasma samples of healthy volunteers and patients with chronic kidney disease. All the measured plasma indoxyl sulfate and 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid concentrations were within the calibration ranges. This novel method may contribute to predicting the activities of drug-metabolizing enzymes and drug transporters in individual patients. 相似文献
997.
Hiroyuki Hayashi Shota Katayama Rong Huang Kosuke Kurushima Isao Tanaka 《固体物理学:研究快报》2015,9(3):192-196
Undoped n‐ and p‐type tin monoxide (SnO) films have been selectively fabricated by pulsed laser deposition with a Sn target and careful control of oxygen partial pressure. The films are epitaxially grown in optimal growth conditions on yttria‐stabilized zirconia (YSZ) substrates with out‐of‐plane and in‐plane orientation relationships of (001)SnO//(001)YSZ and [110]SnO//[100]YSZ, respectively. Both Seebeck and Hall measurements show consistent results on the carrier types of the films. The electron Hall mobility is approximately 11 cm2/Vs at room temperature and the carrier activation energy is 0.14 eV for the n‐type film. The growth at increased oxygen partial pressure yields p‐type films, demonstrating the selective fabrication of both n‐ and p‐type SnO films without doping. (© 2015 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim) 相似文献
998.
999.
Paul W. Dunk Hiroyuki Niwa Hisanori Shinohara Alan G. Marshall 《Molecular physics》2015,113(15-16):2359-2361
Fullerenes have been studied for nearly three decades and enormous advances have been made. Mass spectrometry is commonly used for investigations on the distribution of fullerenes formed from evaporated graphite targets, and soot produced from such targets. We report distributions of fullerenes formed by graphite evaporation by use of a pulsed supersonic cluster source and compare them to certain distributions synthesised by other techniques, such as arc discharge and combustion methods. We highlight the fact that physical processes can occur during the mass spectral analysis of fullerenes under certain conditions that may skew the observed distribution of cage sizes present in a sample. In some cases, an analysis of fullerene-containing soot can greatly exaggerate the relative abundance of large fullerenes compared to C60 and medium-sized fullerenes, depending on the particular experimental setup. 相似文献
1000.
Of the many types of catalysis involving two or more catalysts, synergistic catalysis is of great interest because novel reactions or reaction pathways may be discovered when there is synergy between the catalysts. Herein, we describe a synergistic cascade catalysis, in which immobilized Au/Pd bimetallic nanoparticles and Lewis acids work in tandem to achieve the N-alkylation of primary amides to secondary amides with alcohols via hydrogen autotransfer. When Au/Pd nanoparticles were used with metal triflates, a significant rate acceleration was observed, and the desired secondary amides were obtained in excellent yields. The metal triflate is thought to not only facilitate the addition of primary amides to aldehydes generated in situ, but also enhance the returning of hydrogen from nanoparticles to hydrogen-accepting intermediates. This resulted in a more rapid turnover of the nanoparticle catalyst, and ultimately translated into an increase in the overall rate of the reaction. The two catalysts in this co-catalytic system work in a synergistic and cascade fashion, resulting in an efficient hydrogen autotransfer process. 相似文献